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Oral Enzastaurin in Participants With Relapsed Mantle Cell Lymphoma

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Status and phase

Completed
Phase 2

Conditions

Mantle-Cell Lymphoma

Treatments

Drug: enzastaurin

Study type

Interventional

Funder types

Industry

Identifiers

NCT00088205
H6Q-MC-JCAO (Other Identifier)
8360

Details and patient eligibility

About

The purposes of this study are to determine the safety of oral enzastaurin and any side effects that might be associated with it and whether enzastaurin can help participants with mantle cell lymphoma.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Mantle cell lymphoma
  • Previous treatment for mantle cell lymphoma
  • Previously relapsed mantle cell lymphoma with no more than 4 chemotherapy regimens.
  • Have discontinued all previous therapies for cancer, except corticosteroids up to 25 milligrams per day (mg/day)
  • Adequate organ function

Exclusion criteria

  • Inability to swallow tablets
  • Must not have significant heart problems

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

A
Experimental group
Treatment:
Drug: enzastaurin

Trial contacts and locations

17

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Data sourced from clinicaltrials.gov

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